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Published on: January 7, 2016
Thyroid function during the first year of recombinant human growth hormone therapy in short stature children
Insights
Recombinant human growth hormone (rhGH) treatment may cause temporary thyroid function changes in children, potentially unmasking subclinical hypothyroidism. These transient thyroid shifts do not impact growth velocity during the first year of rhGH therapy.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Therapy
- Thyroid Function Tests
Background:
- The impact of recombinant human growth hormone (rhGH) on thyroid function is debated, with theories suggesting it unmasks central hypothyroidism or induces subclinical primary hypothyroidism.
- Understanding these effects is crucial for monitoring children undergoing rhGH treatment.
Purpose of the Study:
- To evaluate thyroid function changes in children with short stature during their first year of rhGH treatment.
- To assess the correlation between these thyroid function alterations and growth velocity.
Main Methods:
- The study included 37 children receiving rhGH treatment, with 5 excluded due to side effects.
- Thyroid function (TSH, fT4) and growth parameters (height, height velocity) were monitored over the first year.
Main Results:
- A minor TSH increase and no significant fT4 change were observed in most groups within 3-6 months.
- Growth hormone deficiency (GHD) patients showed a significant fT4 decrease without TSH increase.
- Thyroid function normalized by the end of the first year; height velocities were similar across groups, except for GHD patients.
Conclusions:
- Transient subclinical primary hypothyroidism may be unmasked by rhGH therapy, indicated by slight TSH elevation and fT4 decrease.
- These temporary thyroid function changes do not adversely affect growth velocity in the initial year of rhGH treatment.
Introduction:
The relationship between rhGH treatment and thyroid function has been the subject of numerous studies. Some say that rhGH treatment unmasks central hypothyroidism, other say that rhGH induces subclinical primary hypothyroidism.
Aim:
To assess the changes in thyroid function in short stature children in the first year of treatment with rhGH and the impact on growth velocity.
Material And Methods:
We evaluated 37 patients treated with rhGH, 5 were excluded because developed side effects during treatment. We measured height, height velocity, and height standard deviation gain during treatment and thyroid function during the first year of treatment.
Results:
We observed a slight increase in the TSH level and no significant change in the f T4 level after the first 3-6 months of treatment in all the groups; in GH deficiency (GHD) patients, we observed a statistically significant decrease of the f T4 level after the first 3-6 months, without a significant increase of the TSH level. After the first year, thyroid function returned to baseline. There were no differences between height velocities in all the groups, except from the GHD patients.
Conclusions:
The slight increase in the TSH level and the decrease of f T4 level might unmask a transient subclinical primary hypothyroidism but these changes do not influence the growth velocity in first year of rhGH treatment.
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